Outcome and cost analysis of implementing selective Coombs testing in the newborn nursery

Objective:(1) to determine whether infants born to o+ mothers who had selective cord-blood testing would have higher rates of clinically significant hyperbilirubinemia compared with those newborns who had routine cord-blood testing. (2) to determine the amount of cost savings by implementing a policy of selective cord-blood testing in newborns born to o+ mothers.study design:we conducted a retrospective pre/post intervention chart review on all infants in the normal newborn nursery at loyola, born to blood type o+ women between 1 april 2008 and 1 april 2009. the pre-intervention group (routine testing) included infants born within 6 months before implementation of a new policy. the post-intervention group (selective testing) included infants born within 6 months following the implementation of a new policy. data were collected for each of these groups regarding clinically significant hyperbilirubinemia.result:all 250 of the infants in the routine testing group had a cord-blood type and coombs done, whereas 42 of 164 (25%) infants in the selective group had testing done. by the end of the 6 months following the policy change, only 8% of infants were undergoing cord testing. when comparing routine vs selective testing, there was no statistically significant difference in the 24-h serum bilirubin, rate of phototherapy during the birth hospitalization, rate of readmission for hyperbilirubinemia or peak serum bilirubin level at readmission. the 92% reduction of cord-blood typing and coombs testing would lead to a cost saving of $4100 per year to our hospital and $18 900 per year to our patients, and 95 h per year of technician time to perform these tests. when extrapolated to illinois births in 2008, this would lead to an annual cost saving of almost $800 000 to illinois hospitals and about $3.6 million to patients.conclusion:selective newborn cord testing of infants born to o+ mothers can decrease the use of resources and costs without increasing the risk of clinically significant hyperbilirubinemia.